ID

38496

Description

Care China-Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00938119

Lien

https://clinicaltrials.gov/show/NCT00938119

Mots-clés

Versions (1)
  1. 22/10/2019 22/10/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

22 octobre 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00938119

Anglais

Eligibility Cardiovascular Disease NCT00938119

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients between the ages of 18 and 80 (inclusive) receiving cypher select™+
Description

Age | Other Coding | Sirolimus drug-eluting stent Trademark name Specified

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C3846158
UMLS CUI [3,1]
C2199093
UMLS CUI [3,2]
C3242373
UMLS CUI [3,3]
C0205369
sirolimus-eluting coronary stent according to standard clinical practice when financially feasible
Description

Sirolimus drug-eluting stent Coronary

Type de données

boolean

Alias
UMLS CUI [1,1]
C2199093
UMLS CUI [1,2]
C1522318
the patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate institutional review board/ethics committee of the respective clinical site.
Description

Protocol Compliance | Protocol Compliance Legal Guardian | Informed Consent | Informed Consent Legal Guardian

Type de données

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C0023226
UMLS CUI [3]
C0021430
UMLS CUI [4,1]
C0021430
UMLS CUI [4,2]
C0023226
patient has diagnosis of diabetes or is diagnosed with it before or during the index procedure hospitalization based on disease diagnosis criteria
Description

Diabetes Mellitus | Hospitalization

Type de données

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0019993
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any contraindication to any of the following medications: aspirin, heparin, thienopyridines (clopidogrel/ticlopidine), stainless steel, contrast agents, or sirolimus
Description

Medical contraindication Aspirin | Medical contraindication Heparin | Medical contraindication Thienopyridines | Medical contraindication Clopidogrel | Medical contraindication Ticlopidine | Medical contraindication Stainless Steel | Medical contraindication Contrast Media | Medical contraindication Sirolimus

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0019134
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C2936588
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C0070166
UMLS CUI [5,1]
C1301624
UMLS CUI [5,2]
C0040207
UMLS CUI [6,1]
C1301624
UMLS CUI [6,2]
C0038126
UMLS CUI [7,1]
C1301624
UMLS CUI [7,2]
C0009924
UMLS CUI [8,1]
C1301624
UMLS CUI [8,2]
C0072980
an elective surgical procedure is planned that would necessitate interruption of antiplatelet drugs during the first 6 months post enrollment
Description

Elective Surgical Procedure Planned | Requirement Interruption Antiplatelet Agents

Type de données

boolean

Alias
UMLS CUI [1,1]
C0206058
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C1514873
UMLS CUI [2,2]
C1512900
UMLS CUI [2,3]
C0085826
cardiogenic shock
Description

Shock, Cardiogenic

Type de données

boolean

Alias
UMLS CUI [1]
C0036980
terminal illness with life expectancy <1 year
Description

Terminal illness | Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0679247
UMLS CUI [2]
C0023671
st-segment elevation myocardial infarction within 7 days prior to the index procedure
Description

ST segment elevation myocardial infarction

Type de données

boolean

Alias
UMLS CUI [1]
C1536220
any patient who received coronary stent(s) within 1 year
Description

Coronary stent Received Recently

Type de données

boolean

Alias
UMLS CUI [1,1]
C0687568
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0332185
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Similar models

Eligibility Cardiovascular Disease NCT00938119

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age | Other Coding | Sirolimus drug-eluting stent Trademark name Specified
Item
patients between the ages of 18 and 80 (inclusive) receiving cypher select™+
boolean
C0001779 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
C2199093 (UMLS CUI [3,1])
C3242373 (UMLS CUI [3,2])
C0205369 (UMLS CUI [3,3])
Sirolimus drug-eluting stent Coronary
Item
sirolimus-eluting coronary stent according to standard clinical practice when financially feasible
boolean
C2199093 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
Protocol Compliance | Protocol Compliance Legal Guardian | Informed Consent | Informed Consent Legal Guardian
Item
the patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate institutional review board/ethics committee of the respective clinical site.
boolean
C0525058 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C0023226 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3])
C0021430 (UMLS CUI [4,1])
C0023226 (UMLS CUI [4,2])
Diabetes Mellitus | Hospitalization
Item
patient has diagnosis of diabetes or is diagnosed with it before or during the index procedure hospitalization based on disease diagnosis criteria
boolean
C0011849 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Aspirin | Medical contraindication Heparin | Medical contraindication Thienopyridines | Medical contraindication Clopidogrel | Medical contraindication Ticlopidine | Medical contraindication Stainless Steel | Medical contraindication Contrast Media | Medical contraindication Sirolimus
Item
any contraindication to any of the following medications: aspirin, heparin, thienopyridines (clopidogrel/ticlopidine), stainless steel, contrast agents, or sirolimus
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0019134 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C2936588 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C0070166 (UMLS CUI [4,2])
C1301624 (UMLS CUI [5,1])
C0040207 (UMLS CUI [5,2])
C1301624 (UMLS CUI [6,1])
C0038126 (UMLS CUI [6,2])
C1301624 (UMLS CUI [7,1])
C0009924 (UMLS CUI [7,2])
C1301624 (UMLS CUI [8,1])
C0072980 (UMLS CUI [8,2])
Elective Surgical Procedure Planned | Requirement Interruption Antiplatelet Agents
Item
an elective surgical procedure is planned that would necessitate interruption of antiplatelet drugs during the first 6 months post enrollment
boolean
C0206058 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C1512900 (UMLS CUI [2,2])
C0085826 (UMLS CUI [2,3])
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Terminal illness | Life Expectancy
Item
terminal illness with life expectancy <1 year
boolean
C0679247 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
ST segment elevation myocardial infarction
Item
st-segment elevation myocardial infarction within 7 days prior to the index procedure
boolean
C1536220 (UMLS CUI [1])
Coronary stent Received Recently
Item
any patient who received coronary stent(s) within 1 year
boolean
C0687568 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
Retour au début de la page 

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